Gene: PRAME
Official Full Name: PRAME nuclear receptor transcriptional regulatorprovided by HGNC
Gene Summary: This gene encodes an antigen that is preferentially expressed in human melanomas and that is recognized by cytolytic T lymphocytes. It is not expressed in normal tissues, except testis. The encoded protein acts as a repressor of retinoic acid receptor, and likely confers a growth advantage to cancer cells via this function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00056 | PRAME Knockout cell line (A-375) | Human | PRAME | Negative | Online Inquiry | |
KO00198 | PRAME Knockout cell line (HCT 116) | Human | PRAME | 1:2~1:4 | Negative | Online Inquiry |
KO29182 | PRAME Knockout cell line (HeLa) | Human | PRAME | 1:3~1:6 | Negative | Online Inquiry |
KO29183 | PRAME Knockout cell line (HEK293) | Human | PRAME | 1:3~1:6 | Negative | Online Inquiry |
KO29184 | PRAME Knockout cell line (A549) | Human | PRAME | 1:3~1:4 | Negative | Online Inquiry |
PRAME Gene Knockout Cell Lines are sophisticated biological research tools specifically engineered to facilitate the study of the Preferentially Expressed Antigen in Melanoma (PRAME) gene by completely disabling its expression in various cell line backgrounds. Utilizing the CRISPR/Cas9 gene-editing technology, these cell lines allow researchers to delineate the functional role of PRAME in cancer biology and potential therapeutic responses, creating an invaluable resource for both basic and translational research.
The primary function of PRAME Gene Knockout Cell Lines is to enable the comprehensive analysis of the PRAME gene's influence on cellular behaviors such as proliferation, differentiation, and apoptosis. By knocking out the PRAME gene, researchers can observe the resultant phenotypic changes and dissect the molecular pathways in which PRAME is involved. This capability is critical in understanding PRAME’s role in melanoma development and progression, as well as its potential as a target for immunotherapy.
Scientifically, the importance of these knockout cell lines is underscored by their applicability in both research and clinical settings. They serve as vital models for pre-clinical studies aimed at exploring PRAME's involvement in immune response and tumorigenesis, ultimately contributing to the development of targeted therapies. Furthermore, they can play a crucial role in biomarker discovery, aiding in the identification of patient populations that may uniquely benefit from PRAME-targeted treatments.
Compared to alternative models, such as non-specific cell lines or those with incomplete knockouts, PRAME Gene Knockout Cell Lines provide a powerful and precise experimental platform. Their complete gene knockout allows for unequivocal results and enhances data reliability in experimental outcomes. Additionally, these cell lines can be adapted to simulate various microenvironments and conditions, providing flexibility in experimental design.
For researchers and clinicians looking to advance their work in cancer biology and therapeutic development, PRAME Gene Knockout Cell Lines represent an indispensable resource. By leveraging these tools, users can gain critical insights into the mechanisms of PRAME in tumor behavior, supporting the development of innovative approaches in patient care.
Our company specializes in the development of high-quality, functional cellular models for research purposes, backed by extensive expertise in gene editing technologies and cancer biology. We are committed to empowering scientific discovery through our innovative product offerings, ensuring researchers have access to the precise tools they need to drive their studies forward.
Please note that all services are for research use only. Not intended for any clinical use.
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